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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21949Generated: October 24, 2026

Triethylamine → 4-(2-Ethoxybenzamido)-1-methyl-3-propylpyrazole-5-carboxamide

https://huagongshe.com/en/reaction/21949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Ethoxybenzoyl chlorideHCID 3016397—
Reactant4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamideHCID 3338044—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-(2-Ethoxybenzamido)-1-methyl-3-propylpyrazole-5-carboxamideHCID 85013540.6%

Reaction Steps

A solution of 2-ethoxybenzoyl chloride (6.1 g, 33.0 mmol) in dichloromethane (50 ml) was added to a stirred solution of 4-amino-1-methyl-3-n-propylpyrazole-5-carboxamide (3.0 g, 16.4 mmol), 4-dimethylaminopyridine (0.02 g, 0.164 mmol) and triethylamine (3.34 g, 33.0 mmol) in dichloromethane (50 ml) at 0° C. The resulting mixture was allowed to warm to room temperature and stirred for a further 2 hours. The solvent was evaporated under vacuum, the residue dissolved in a 19:1 mixture of dichloromethane and methanol (250 ml), and then the solution washed with 1N hydrochloric acid (100 ml), dried (MgSO4) and evaporated under vacuum. The crude material was chromatographed on silica gel (200 g), eluting with a 97:3 mixture of dichloromethane and methanol, to give a pink solid; crystallisation from ethyl acetate-hexane gave the pyrazole-5-carboxamide as a pale pink solid (2.2 g, 40%), m.p. 153°-155° C. Found: C,61.66; H,6.77; N,16.95. C17H22N4O3 requires C,61.80; H,6.71; N,16.96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426107
Source datasetuspto-grants-1995_06
ORD IDord-4999417e4e2e4bd6b7bbf1c5b481875b
Source noteuspto-grants-1995_06